Nass Norbert, Ignatov Atanas, Andreas Ludwig, Weißenborn Christine, Kalinski Thomas, Sel Saadettin
Department of Pathology, Otto von Guericke University Magdeburg, Leipziger Str. 44, House 28, 39120, Magdeburg, Germany.
Department of Obstetrics and Gynecology, Otto von Guericke University Magdeburg, Gerhart-Hauptmann Str. 35, 39108, Magdeburg, Germany.
Histochem Cell Biol. 2017 May;147(5):625-634. doi: 10.1007/s00418-016-1534-4. Epub 2016 Dec 23.
Advanced glycation end products (AGEs) accumulate as a result of high concentrations of reactive aldehydes, oxidative stress, and insufficient degradation of glycated proteins. AGEs are therefore accepted biomarkers for aging, diabetes, and several degenerative diseases. Due to the Warburg effect and increased oxidative stress, cancer cells frequently accumulate significant amounts of AGEs. As the accumulation of AGEs may reflect the metabolic state and receptor signaling, we evaluated the potential prognostic and predictive value of this biomarker. We used immunohistochemistry to determine the AGE Nε-carboxymethyl lysine (CML) in 213 mammary carcinoma samples and Western blotting to detect AGEs in cell cultures. Whereas no significant correlation between hormone receptor status and CML was observed in cell lines, CML accumulation in tumors was positively correlated with the presence of estrogen receptor alpha, the postmenopausal state, and age. A negative correlation was found for grade III carcinomas and triple-negative cases. In a retrospective Kaplan-Meier survival analysis, there was a statistical trend that high CML accumulation correlated with a more favorable prognosis (relapse-free survival, RFS) under tamoxifen treatment (p = 0.1). In estrogen receptor-negative cases, the high CML content was significantly correlated with an unfavorable outcome (RFS) of chemotherapy (p = 0.046). CML is a therefore a potentially predictive marker for the treatment of breast cancer patients with tamoxifen or chemotherapy.
晚期糖基化终末产物(AGEs)因高浓度的活性醛、氧化应激以及糖化蛋白降解不足而积累。因此,AGEs被公认为衰老、糖尿病和几种退行性疾病的生物标志物。由于瓦伯格效应和氧化应激增加,癌细胞经常积累大量的AGEs。鉴于AGEs的积累可能反映代谢状态和受体信号,我们评估了这种生物标志物的潜在预后和预测价值。我们使用免疫组织化学法测定213例乳腺癌样本中的AGE Nε-羧甲基赖氨酸(CML),并使用蛋白质印迹法检测细胞培养物中的AGEs。虽然在细胞系中未观察到激素受体状态与CML之间存在显著相关性,但肿瘤中CML的积累与雌激素受体α的存在、绝经后状态和年龄呈正相关。在III级癌和三阴性病例中发现呈负相关。在一项回顾性Kaplan-Meier生存分析中,有统计学趋势表明,在他莫昔芬治疗下,高CML积累与更有利的预后(无复发生存期,RFS)相关(p = 0.1)。在雌激素受体阴性的病例中,高CML含量与化疗的不良结局(RFS)显著相关(p = 0.046)。因此,CML是他莫昔芬或化疗治疗乳腺癌患者的一个潜在预测标志物。